Clinical Research Associate, Sponsor Dedicated

Durham, North Carolina, United States of America

Aurora, Illinois, United States

San Fernando, California, United States

Clinton, Missouri, United States

Mansfield, Ohio, United States

Santa Cruz, California, United States

Santa Fe, New Mexico, United States

South Shore, Illinois, United States

Elk Grove, California, United States

Hudson, Ohio, United States

Englewood, Colorado, United States

Bellingham, Washington, United States

Marysville, Washington, United States

Overland Park, KS, United States of America

Evanston, Wyoming, United States

La Habra, California, United States

Prescott, Arizona, United States

Westchester, New York, United States

Mount Vernon, Illinois, United States

Warren, Ohio, United States of America

Linden, New Jersey, United States

Fremont, California, United States

Del Mar, California, United States

Lake Tahoe, California, United States

Northfield, New Jersey, United States

Fort Pierce, Florida, United States

Wilkes Barre, Pennsylvania, United States

Camden, New Jersey, United States

Lancaster, California, United States

Clarksville, Tennessee, United States

Adair, Iowa, United States

Fort Collins, Colorado, United States

Breckenridge, Colorado, United States

Littleton, Colorado, United States

Liverpool, New York, United States

Ft Lauderdale, Florida, United States

Springfield, Ohio, United States

Long Island, New York, United States

Gloucester, Virginia, United States

West Point, Virginia, United States

O'Fallon, Illinois, United States

Cheyenne, Wyoming, United States

Manhattan, New York, United States

New City, New York, United States

Parsippany, New Jersey, United States of America

Queens, New York, United States

New York City, New York, United States

Escondido, California, United States

Oak Brook, Illinois, United States

Merritt Island, Florida, United States

El Cajon, California, United States

Ontario, California, United States

Afton, Wyoming, United States

Abilene, Texas, United States

Orangevale, California, United States

Abingdon, Virginia, United States

Orland Park, Illinois, United States

Shenandoah, Texas, United States

Akron, Ohio, United States

Paradise Valley, Arizona, United States

Newark, Delaware, United States

Hollywood, Florida, United States

Port Saint Lucie, Florida, United States

Lawton, Oklahoma, United States

Portland, Oregon, United States

Chino Hills, California, United States

Belmar, New Jersey, United States

Sonora, California, United States

Berkley, California, United States

Springfield, Massachusetts, United States

Springfield, Missouri, United States

San Jose, California, United States

Beverly Hills, California, United States

Melbourne, Florida, United States

Colorado Springs, Colorado, United States

St. Petersburg, Florida, United States

Panama City, Florida, United States

Redondo Beach, California, United States

Crystal Lake, Illinois, United States

Rochester, New York, United States

Ada, Oklahoma, United States

Kansas City, Missouri, United States

Ainsworth, Nebraska, United States

Carlsbad, CA, United States of America

Denver , Colorado, United States

Full time

R1541733

To be eligible for this position, you must reside in the same country where the job is located.

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site…